Not yet recruitingPHASE1, PHASE2NCT07339163
Efficacy of Booster Injection With Gardasil-9 Vaccine on Intersurgical Interval* for Adults With Recurrent Respiratory Papillomatosis*
Studying Recurrent respiratory papillomatosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Ohio State University
- Principal Investigator
- Laura Matrka, Doctor of MedicineOhio State University
- Intervention
- GARDASIL®9 (Human Papillomavirus 9-valent Vaccine, Recombinant)(biological)
- Enrollment
- 50 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2026 – 2035
Study locations (1)
- Department of Otolaryngology - Head & Neck Surgery, Columbus, Ohio, United States
Collaborators
Merck Sharp & Dohme LLC
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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